A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv750271



Internal ID15697541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72243964..72286159hg38UCSC Ensembl
Innerchr10:74003722..74045917hg19UCSC Ensembl
Innerchr10:73673728..73715923hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3842196
hg1942196
hg1842196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551514
Supporting Variants
Samples
Known GenesDDIT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv750271
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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